(Q52057993)

English

Phocomelia and additional anomalies in two sisters.

scientific article published in May 1990

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Statements

scholarly article

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

Phocomelia and additional anomalies in two sisters. (English)

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

author name string

A Schinzel

1

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

publication date

1 May 1990

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

84

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

6

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

539-541

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

https://scigraph.springernature.com/pub.10.1007/bf00210806

0 references

A new syndrome of severe upper limb hypoplasia and Müllerian duct anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Limb deficiency and splenogonadal fusion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The SC phocomelia syndrome: Report of two cases with cytogenetic abnormality

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Roberts syndrome and SC phocomelia. A single genetic entity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The CHILD syndrome. Congenital hemidysplasia with ichthyosiform erythroderma and limb defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The thalidomide syndrome: risks of exposure and spectrum of malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital diaphragmatic hernia associated with homolateral upper limb malformation: A study of possible pathogenesis in four cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndrome of multiple congenital malformations including phocomelia, thrombocytopenia, encephalocele, and urogenital abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338339

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00210806

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

1 reference

Europe PubMed Central

20 April 2018

http://europepmc.org/abstract/MED/2338339

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